Staff Biostatistician (Clinical Validation)
作为一名工作人员生物统计师,你将利用自己的强大的应用统计数据,IVD 和临床研究专业知识来推动脏病和其他优先基因项目的临床验证研究战略,设计,分析和解释。主要责任:·战略研究设计和分析:独立领导临床验證研究的设计,分析与解释以支持体外诊断批准 (例如 CDx,510k),PMA 等) ·监管合规:确保统计方法和分析符合监管机构 (如 FDA)所设定的标准。与监管部门进行统计互动。· 文件和报告:为跨职业和外部合作者和利益相关者准备全面的统计分析协议 (SAP),报告和演示。· 跨职能领导:作为优先项目团队的统计领先人员。与临床科学,数据管理和产品团队合作,将统计专业知识集成到项目的规划和执行中。识别风险,沟通关切并倡导解决方案。·临床研究及其他领域:推动高影响性的临床试验,研究和出版物的设计与执行,促进我们世界级产品组合的发展 · 保持生物统计学和临床验证方法技术方面的进展情况最新,实施创新方法来支持诊断产品开发和监管提交 · 导师并向年轻团队成员提供技术监督资格:· 教育:博士或士学位在生物统计,统计学或相关领域 ·经验:· 至少8年的相关行业经验,最好是在分子诊断,生物技术或相关领域。· 在监管环境中经验证明,包括以前的 CDx 或 IVD 提交经验 · 具有下一代测序 (NGS),遗传和/或基因线相关数据的经验。·与 R 统计分析软件至少有4年的实践经验:KNOWLEDGE, SKILLS, AND ABILITIES: · 专家对诊断医学中的统计方法实操了解,包括了解 FDA 指南 · 前任经验互动性药物
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This is an exciting opportunity to advance Natera’s regulated product portfolio of cutting-edge molecular diagnostic tests. As a Staff Biostatistician, you will leverage your strong applied statistics, IVD, and Clinical Research expertise to drive the strategy, design, analysis, and interpretation of clinical validation studies for kidney disease and other high-priority germline projects.
PRIMARY RESPONSIBILITIES:
- Strategic Study Design and Analysis: Independently lead the design, analysis, and interpretation of clinical validation studies to support in vitro diagnostic approvals (e.g., CDx, 510(k), PMA, etc.)
- Regulatory Compliance: Ensure statistical methodologies and analyses meet the standards set by regulatory agencies such as FDA. Drive statistical interactions with regulatory authorities.
- Documentation and Reporting: Prepare comprehensive statistical analysis protocols (SAPs), reports, and presentations for cross-functional and external collaborators and stakeholders.
- Cross-Functional Leadership: Serve as the statistical lead on high-priority project teams. Partner with Clinical Science, Data Management, and Product teams to integrate statistical expertise into project planning and execution. Identify risks, communicate concerns, and champion solutions to interdisciplinary project teams
- Clinical Research and Beyond: Drive design and execution of high-impact research clinical trials, studies, and publications that push the development of our world-class product portfolio
- Stay current with advancements in Biostatistics and clinical validation methodology, implementing innovative approaches to support diagnostic product development and regulatory submissions
- Mentor and provide technical supervision to junior team members
QUALIFICATIONS:
- Education: Ph.D. or Master's degree in Biostatistics, Statistics, or a related field
- Experience:
- At least 8 years of relevant industry experience, preferably within molecular diagnostics, biotechnology, or related fields.
- Demonstrated experience in regulated environments, including previous CDx or IVD submission experience
- Experience with next-generation sequencing (NGS), genetic, and/or germline-related data.
- Minimum of 4 years practical experience with R statistical analysis software
KNOWLEDGE, SKILLS, AND ABILITIES:
- Expert working knowledge of statistical methodology in diagnostic medicine, including an understanding of FDA guidelines
- Previous experience interacting with regulatory bodies such as the FDA.
- Demonstrated ability and enthusiasm for working on cross-functional teams with members of diverse technical backgrounds
- Strong track record of producing high quality written documentation for multiple audiences
- Prior experience with germline assay development preferred
- Prior experience with kidney disease desired
- Experience in design and analyses of clinical validation studies
- Strong communication skills, with the ability to explain complex statistical concepts to non-statistical audiences.
- Attention to detail and a commitment to delivering high-quality work under tight deadlines.
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.
Remote USA
$164,000—$205,000 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit www.natera.com.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
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Link: https://www.natera.com/notice-of-data-collection-california-residents/
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